Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q4K9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.528 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.459 |
DOC_ANK_TNKS_1 | 236 | 243 | PF00023 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.425 |
DOC_MAPK_MEF2A_6 | 225 | 233 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.464 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.539 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.433 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 207 | 215 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 306 | 316 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 376 | 382 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.583 |
LIG_14-3-3_CterR_2 | 404 | 408 | PF00244 | 0.676 |
LIG_APCC_ABBA_1 | 195 | 200 | PF00400 | 0.495 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.628 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.604 |
LIG_BIR_III_4 | 92 | 96 | PF00653 | 0.388 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.571 |
LIG_Clathr_ClatBox_1 | 279 | 283 | PF01394 | 0.320 |
LIG_EH_1 | 42 | 46 | PF12763 | 0.504 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.446 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.453 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.568 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.346 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.515 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.408 |
LIG_Integrin_RGD_1 | 340 | 342 | PF01839 | 0.579 |
LIG_Integrin_RGD_1 | 40 | 42 | PF01839 | 0.501 |
LIG_LIR_Gen_1 | 104 | 115 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 159 | 167 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.531 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.374 |
LIG_PCNA_yPIPBox_3 | 17 | 27 | PF02747 | 0.554 |
LIG_PCNA_yPIPBox_3 | 185 | 194 | PF02747 | 0.387 |
LIG_REV1ctd_RIR_1 | 278 | 288 | PF16727 | 0.314 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.616 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.620 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.388 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.642 |
LIG_SUMO_SIM_anti_2 | 22 | 29 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 226 | 232 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 34 | 40 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 244 | 249 | PF11976 | 0.399 |
MOD_CDC14_SPxK_1 | 401 | 404 | PF00782 | 0.679 |
MOD_CDK_SPxK_1 | 398 | 404 | PF00069 | 0.664 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.388 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.481 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.388 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.528 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.378 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.452 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.595 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.645 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.388 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.563 |
MOD_GlcNHglycan | 92 | 96 | PF01048 | 0.388 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.315 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.465 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.471 |
MOD_LATS_1 | 375 | 381 | PF00433 | 0.545 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.388 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.312 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.321 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.398 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.381 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.550 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.631 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.501 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.519 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.632 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.510 |
MOD_PKB_1 | 89 | 97 | PF00069 | 0.340 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.367 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.436 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.415 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.381 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.467 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.457 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.466 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.414 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.430 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.460 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.609 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.302 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.577 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.525 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 353 | 357 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.340 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 88 | 91 | PF00400 | 0.291 |
TRG_NES_CRM1_1 | 278 | 292 | PF08389 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBF8 | Leptomonas seymouri | 52% | 100% |
A0A3Q8IHJ7 | Leishmania donovani | 93% | 100% |
A4HL51 | Leishmania braziliensis | 74% | 100% |
A4I8N0 | Leishmania infantum | 93% | 100% |
E9B3J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |